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Parexel

End-to-end clinical trials and regulatory consulting

Enrollment Coordinator - English and Korean Fluent

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeGlendale, CA, USA

About the Job

Requirements

  • Two years of experience in clinical research enrollment and/or experience as a coordinator in either early-phase or late-phase clinical trials.
  • A Bachelor's degree; equivalent relevant work experience will also be considered.
  • Fluency in English and Korean, both written and verbal.

Responsibilities

  • Screen potential clinical trial volunteers according to protocol-specific requirements and CFR/ICH Good Clinical Practice guidelines, ensuring all study laboratory and medical tests are completed and eligibility requirements for assigned studies are met.
  • Ensure all established timelines relating to the area of responsibility and assigned projects are met.
  • Ensure completion of enrollment for assigned studies and closely manage the process to minimize waste.
  • Ensure quality control performance of all electronic and paper source documents.
  • Assist in reviewing Informed Consent Documents, Study Protocols, Source Documents, and Case Report Forms during development.
  • Ensure screening ratios and marketing expenditures are maintained within study-specific budgets.
  • Participate in team project meetings and provide regular updates for assigned studies.
  • Develop and present training material to department staff for assigned studies.
  • Arrange for pre- and post-procedure laboratory work and initiate follow-up as required.
  • Ensure follow-up to all queries related to screening and enrollment of assigned studies.
  • Collect, organize, and prepare data for physician review, and assist physicians with completing flow sheets in medical records and progress notes.
  • Enter data into the database when required; ensure all paper source documents are completed as required by protocol; and update and maintain the Clinical Study File.
  • Support Standard Operating Procedures, Good Clinical Practices, and all work processes to ensure efficient and compliant clinical operations of the Early Phase Clinical Unit.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

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